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IBUPROFEN/CODEINE-TIH 200/12.8 tablet blister pack - TGA Drug Approval Details
Approvals
/
TGA
/
IBUPROFEN/CODEINE-TIH 200/12.8 tablet blister pack
Approved
STANDARD
IBUPROFEN/CODEINE-TIH 200/12.8 tablet blister pack
Arrotex Pharmaceuticals Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
1a74f45e90ddc200
Company
Arrotex Pharmaceuticals Pty Ltd
Type
Standard
Approval Details
Approval Id
1a74f45e90ddc200
Product Name
IBUPROFEN/CODEINE-TIH 200/12.8 tablet blister pack
Artg Id
158210
Artg Name
IBUPROFEN/CODEINE-TIH 200/12.8 tablet blister pack
Sponsor
Arrotex Pharmaceuticals Pty Ltd
Company Detail Path
/organization/arrotex-pharmaceuticals-pty-ltd
Artg Date
2008-12-23
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/c88b308e34081d213a39089f45cfbf74.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/242dea98927417482515f8374390df22.pdf
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
1a74f45e90ddc200
Type
Standard
Back to TGA Approvals